Description
AQUACEL FOAM ADHESIVE FORMAT Multi-layered adhesive dressing in polyurethane-hydrocellular foam with alveolar structure, accompanied by a thin layer of hydrophilic contact with the wound bed, an external polyurethane film and a silicone (hypoallergenic) adhesive. The mixed-cell polyurethane layer is highly hydrophilic, absorbent, retaining the exudate and transpiring. The Hydrofiber technology layer in direct contact with the lesion illusions, allows AQUACEL Foam to interact actively with the lesionestessa by instantly forming a soft gel that keeps the environment moist and retains the exudate, promoting healing and reducing the risk of maceration of the cuteperilesional . The breathable outer film promotes the transmission of vapors and gases and creates a waterproof barrier against fluids and bacteria that protects the wound from external contamination. The silicone adhesive edge is extremely delicate to remove, thin and highly-distributable. AQUACEL Foam is indicated for use in poorly to moderately exuding wounds on: Traumatic wounds: small abrasions, tears and small cuts. Chronic wounds: ulcers in the lower limbs (venous ulcers, arterial ulcers and mixed adnexitis ulcers), diabetic ulcers, partial-thickness and all-thickness pressure ulcers. Acute wounds: surgical wounds (left to heal by secondary intention) and cutaneous areas of skin. Oncological wounds: lesions with high exudate (cutaneous mycotic tumors, metastasicutaneous tumors and sarcoma). It can be used both as a primary and a secondary dressing. LATEX FREE- FTALATI FREE. How to use Choose a dressing of shape and size such that the absorbent pad is central to the wider area of the wound. Align the center of the dressing with the wound center and place the central dressing buffer directly over the wound. The dressing must be changed when clinically indicated or when it is saturated exudate; in any case no later than 7 days of stay in situ. AQUACEL Foam can be used as primary medication, or secondary inassociation with other products. Components Sterile dressing consisting of: an external waterproof film in polyurethane, a hydrophilic polyurethane stratum with a thickness of 2.5 mm, density of around 300 g / m2, and a cell size of 200-300 microns, an absorbing layer of non-woven fibers pure sodium carboxymethylcellulose in gelling fibers (NaCMC) surrounded by a thin and delicate silicone adhesive edge. Sterilization method: Sterilized with ethylene oxide. Warnings Testotestotesto. Report any warnings / precautions for use here. storage Protect from light sources, store in a dry place at room temperature (10 ? C – 25 ? C). Validity in years: 3. Maximum time of stay in situ: 7 days. Codicidavailable and methods of presentation / packaging Code Measurements Perconage unit ISO coding CodicePARAF RDM 420804 8x8cm 10 923590158 1236535 / R 420680 10×10 cm 10 09.21.12.003 922859931 1236555 / R 420619 12,5×12,5cm 10 922859943 1236556 / R 420621 17,5×17,5cm 10 922860059 1236565 / R 420623 21×21 cm 5 09.21.12.006 922860061 1236567 / R 420624 25×30 cm 5 922860073 1236569 / R 420625 20x14cm-Heel 5 09.21.12.012 922860085 1236571 / R 420626 20×17 cm-Sacred 5 09.21.12.012 922860097 1236574 / R 420828 24×21.5cm-Sacro 5 09.21.12.012 926550322 1236575 / R 421151 10×20 cm 10 970527990 1377881 / R 421153 10×25 cm 10 970528028 1377882 / R 421155 10×30 cm 10 970528030 1377885 / R Physical characteristics Capacity for managing the exudate in 24h * Total exudate management capacity (TFHC) 11.00 ? 0.09 g / 10 cm? / 24 hrs Retention and absorption under compression * Absorbency (g / g) 10.71 ? 0.54 Retention (g / g) 8.73 ? 0.29 Withholding percentage 81.6 ? 2.5 Board thickness (mm) 0.25 Adhesive edge width (cm) 2 cm * The test was performed according to BS EN13726-1: 2002-Test Methods for Primary Wound Dressing Steam permeability (MVTR) (g / cm 2 ) Absorption capacity (g / cm 2 ) Retention capacity (g / cm 2 ) 24h 0.942 0,496 1,439 48 h 1,914 0.493 2,407 72 h 2,911 0.493 3,404.
